Resources & Insights

Clinical trials are both scientific and deeply personal. This short video reflects the perspective that guides our work in supporting sponsors and patients.

Explore the 11 GCP principles outlined in ICH E6(R3).

What makes rare disease trials unique? Explore perspectives across functions from a rare disease CRO team.

How long does it take to go from final protocol to database go-live?

Associate Director of Medical Writing Samia Khader explores a handful of strategies for expediting CSR delivery.

How can a QA consultant help your team fully adopt QbD?

We spoke with PharPoint’s Director of Quality Assurance to explore what a “quality culture” in the clinical research space entails in practice, beyond just the buzzword.

QA Director Melisa Williamson talks about “Out of the Crisis” by W. Edwards Deming and how it has influenced her approach to quality.

Explore three common findings from a data management consultant who has experience performing DM CRO oversight.

Will you actually be working with the team a CRO introduces you to in early discussions?